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    Wyświetlanie 1-13 z 13
    Tytuł:
    Heme oxygenase-1 expression in disease states.
    Autorzy:
    Deshane, Jessy
    Wright, Marcienne
    Agarwal, Anupam
    Powiązania:
    https://bibliotekanauki.pl/articles/1041399.pdf
    Data publikacji:
    2005
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    heme oxygenase-1
    heme
    cytoprotection
    polymorphisms
    disease
    Opis:
    Heme oxygenase-1 (HO-1) is an enzyme which catalyzes the rate-limiting step in heme degradation resulting in the formation of iron, carbon monoxide and biliverdin, which is subsequently converted to bilirubin by biliverdin reductase. The biological effects exerted by the products of this enzymatic reaction have gained much attention. The anti-oxidant, anti-inflammatory and cytoprotective functions associated with HO-1 are attributable to one or more of its degradation products. Induction of HO-1 occurs as an adaptive and beneficial response to several injurious stimuli including heme and this inducible nature of HO-1 signifies its importance in several pathophysiological disease states. The beneficial role of HO-1 has been implicated in several clinically relevant disease states involving multiple organ systems as well as significant biological processes such as ischemia-reperfusion injury, inflammation/immune dysfunction and transplantation. HO-1 has thus emerged as a key target molecule with therapeutic implications.
    Źródło:
    Acta Biochimica Polonica; 2005, 52, 2; 273-284
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Lysine-specific gingipain K and heme/hemoglobin receptor HmuR are involved in heme utilization in Porphyromonas gingivalis.
    Autorzy:
    Simpson, Waltena
    Olczak, Teresa
    Genco, Caroline
    Powiązania:
    https://bibliotekanauki.pl/articles/1043355.pdf
    Data publikacji:
    2004
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    Kgp
    heme
    Porphyromonas gingivalis
    HmuR
    gingipain
    Opis:
    We have previously reported on the identification and characterization of the Porphyromonas gingivalis A7436 strain outer membrane receptor HmuR, which is involved in the acquisition of hemin and hemoglobin. We demonstrated that HmuR interacts with the lysine- (Kgp) and arginine- (HRgpA) specific proteases (gingipains) and that Kgp and HRgpA can bind and degrade hemoglobin. Here, we report on the physiological significance of the HmuR-Kgp complex in heme utilization in P. gingivalis through the construction and characterization of a defined kgp mutant and a hmuR kgp double mutant in P. gingivalis A7436. The P. gingivalis kgp mutant exhibited a decreased ability to bind both hemin and hemoglobin. Growth of this strain with hemoglobin was delayed and its ability to utilize hemin as a sole iron source was diminished as compared to the wild type strain. Inactivation of both the hmuR and kgp genes resulted in further decreased ability of P. gingivalis to bind hemoglobin and hemin, as well as diminished ability to utilize either hemin or hemoglobin as a sole iron source. Collectively, these in vivo results further confirmed that both HmuR and Kgp are involved in the utilization of hemin and hemoglobin in P. gingivalis A7436.
    Źródło:
    Acta Biochimica Polonica; 2004, 51, 1; 253-262
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Polscy badacze chemii porfiryn. I. Pionierzy
    Polish porphyrin chemists. I. Pioneers
    Autorzy:
    Wojaczyński, Jacek
    Powiązania:
    https://bibliotekanauki.pl/articles/1409971.pdf
    Data publikacji:
    2021
    Wydawca:
    Polskie Towarzystwo Chemiczne
    Tematy:
    chlorofil
    hem
    porfiryna
    chlorophyll
    heme
    porphyrin
    Opis:
    Polish chemists have been engaged in the development of chemistry of porphyrins and related macrocycles. In the first part of the historical review, short biographies and achievements of the pioneers in the field are presented. In particular, the importance of studies performed by Marceli Nencki, Leon Marchlewski, and their co-workers, in the discovery of structures of pigments of life — heme of chlorophyll — is underlined. The contributions of other Polish biochemists and forensic chemists are discussed as well.
    Źródło:
    Wiadomości Chemiczne; 2021, 75, 5-6; 533-551
    0043-5104
    2300-0295
    Pojawia się w:
    Wiadomości Chemiczne
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Evaluation of the activity of thermostable DNA polymerases in the presence of heme, as a key inhibitor in the real time PCR method in diagnostics of sepsis
    Autorzy:
    Gosiewski, Tomasz
    Brzychczy-Włoch, Monika
    Pietrzyk, Agata
    Sroka, Agnieszka
    Bulanda, Małgorzata
    Powiązania:
    https://bibliotekanauki.pl/articles/1039451.pdf
    Data publikacji:
    2013
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    polymerase inhibitor
    heme
    real time PCR
    sepsis
    Opis:
    The study aim was evaluation of the usefulness of several thermostable DNA polymerases in real time PCR conducted in the presence of the heme. Our study had the advantage of testing several different polymerases, one of which proved to be the least sensitive to heme activity. We also found that there is no need of supplementing the reaction mixture with protective substances like BSA. Selection of the appropriate polymerase can increase the efficiency of the PCR reaction which is very important for diagnosis of sepsis and for other analyses performed on DNA template isolated from the blood.
    Źródło:
    Acta Biochimica Polonica; 2013, 60, 4; 603-606
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Heme iron in meat as the main source of iron in the human diet
    Autorzy:
    Buzala, M.
    Slomka, A.
    Janicki, B.
    Powiązania:
    https://bibliotekanauki.pl/articles/1189787.pdf
    Data publikacji:
    2016
    Wydawca:
    Uniwersytet Warmińsko-Mazurski w Olsztynie / Polskie Towarzystwo Magnezologiczne im. Prof. Juliana Aleksandrowicza
    Tematy:
    heme iron
    iron
    meat
    iron source
    human diet
    human nutrition
    Opis:
    Iron is a trace element involved in many cardinal metabolic processes of almost all living organisms. It is well known that iron participates in oxygen transport as well as it is a cofactor in many fundamental enzymatic and nonenzymatic processes. Accordingly, disturbances of iron homeostasis can cause serious clinical consequences. In humans, dietary iron can enter the body in two main forms: heme and nonheme. The former is a component of many hemoproteins (including myoglobin, hemoglobin, cytochromes b and c) and is easily absorbed in the duodenal enterocytes. Red meat is an excellent source of heme iron, while the less bioavailable nonheme form is found in large amounts in milk products and vegetables. For this reason, consumers of meat have a better iron status than vegetarians and vegans. The aim of this paper was to discuss the role of heme iron in the human diet. Heme iron found in muscle protein should be supplied to humans to prevent iron deficiency, which can lead to anemia. It is easily absorbed by the human body and its main source is red meat. In addition, heme iron, which is mainly found in myoglobin in meat, contributes to the desirable bright red color and to the most undesirable brown color of meat. Both heme and nonheme iron are catalysts of lipid oxidation in meat. This process lowers the nutritive value through oxidation of polyunsaturated fatty acids, which produces an undesirable flavor and aroma. The present review is focused on the role of heme iron, which is mainly found in meat and is the principal source of iron in the human diet.
    Źródło:
    Journal of Elementology; 2016, 21, 1; 303-314
    1644-2296
    Pojawia się w:
    Journal of Elementology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Heme iron in meat as the main source of iron in the human diet
    Autorzy:
    Buzala, M.
    Slomka, A.
    Janicki, B.
    Powiązania:
    https://bibliotekanauki.pl/articles/962737.pdf
    Data publikacji:
    2016
    Wydawca:
    Uniwersytet Warmińsko-Mazurski w Olsztynie / Polskie Towarzystwo Magnezologiczne im. Prof. Juliana Aleksandrowicza
    Tematy:
    heme iron
    iron
    meat
    iron source
    human diet
    human nutrition
    Opis:
    Iron is a trace element involved in many cardinal metabolic processes of almost all living organisms. It is well known that iron participates in oxygen transport as well as it is a cofactor in many fundamental enzymatic and nonenzymatic processes. Accordingly, disturbances of iron homeostasis can cause serious clinical consequences. In humans, dietary iron can enter the body in two main forms: heme and nonheme. The former is a component of many hemoproteins (including myoglobin, hemoglobin, cytochromes b and c) and is easily absorbed in the duodenal enterocytes. Red meat is an excellent source of heme iron, while the less bioavailable nonheme form is found in large amounts in milk products and vegetables. For this reason, consumers of meat have a better iron status than vegetarians and vegans. The aim of this paper was to discuss the role of heme iron in the human diet. Heme iron found in muscle protein should be supplied to humans to prevent iron deficiency, which can lead to anemia. It is easily absorbed by the human body and its main source is red meat. In addition, heme iron, which is mainly found in myoglobin in meat, contributes to the desirable bright red color and to the most undesirable brown color of meat. Both heme and nonheme iron are catalysts of lipid oxidation in meat. This process lowers the nutritive value through oxidation of polyunsaturated fatty acids, which produces an undesirable flavor and aroma. The present review is focused on the role of heme iron, which is mainly found in meat and is the principal source of iron in the human diet.
    Źródło:
    Journal of Elementology; 2016, 21, 1
    1644-2296
    Pojawia się w:
    Journal of Elementology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Effects of protoporphyrins on production of nitric oxide and expression of vascular endothelial growth factor in vascular smooth muscle cells and macrophages.
    Autorzy:
    Józkowicz, Alicja
    Dulak, Józef
    Powiązania:
    https://bibliotekanauki.pl/articles/1043649.pdf
    Data publikacji:
    2003
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    cell viability
    metalloporphyrins
    vascular endothelial growth factor
    nitric oxide
    heme oxygenase
    Opis:
    Heme oxygenase-1 (HO-1), an inducible enzyme degrading heme to biliverdin, iron and carbon monoxide, is involved in regulation of inflammation and angiogenesis. Tin protoporphyrin (SnPPIX) and zinc protoporphyrin (ZnPPIX) are commonly used as competitive inhibitors of HO-1. We aimed to compare the effects of SnPPIX and ZnPPIX on the production of vascular endothelial growth factor (VEGF), activity of inducible nitric oxide synthase (iNOS) and cell viability. All experiments were performed on rat vascular smooth muscle cells and murine RAW264.7 macrophages treated with 3-10 μM protoporphyrins. Some cells were additionally stimulated with IL-1β or with lipopolysaccharide. After a 24 h incubation period SnPPIX and ZnPPIX significantly reduced the generation of VEGF in vascular smooth muscle cells and RAW264.7, both in resting and stimulated cells. The inhibitory potentials of both protoporphyrins on VEGF synthesis were very similar. In contrast, analysis of iNOS activity revealed that results obtained with different HO-1 inhibitors are discrepant. Generation of nitric oxide by iNOS was significantly increased by SnPPIX but strongly decreased by ZnPPIX. Similar differences were observed when cell viability was compared. SnPPIX improved the cell survival rate, whereas the same doses of ZnPPIX exerted some cytotoxic effects. In summary, SnPPIX and ZnPPIX can be used as HO-1 inhibitors in some experimental models. However, these compounds produce also HO-independent effects, which can make the interpretation of experiments very uncertain. Thus the involvement of the HO-1 pathway should be always confirmed by more specific methods.
    Źródło:
    Acta Biochimica Polonica; 2003, 50, 1; 69-79
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Hem12, an enzyme of heme biosynthesis pathway, is monoubiquitinated by Rsp5 ubiquitin ligase in yeast cells
    Autorzy:
    Chelstowska, Anna
    Jastrzebska, Zaneta
    Kaminska, Joanna
    Sadurska, Anna
    Plochocka, Danuta
    Rytka, Joanna
    Zoladek, Teresa
    Powiązania:
    https://bibliotekanauki.pl/articles/1038993.pdf
    Data publikacji:
    2015
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    yeast
    heme biosynthesis
    Hem12
    ubiquitination
    Rsp5 ligase
    protein degradation
    Opis:
    Heme biosynthesis pathway is conserved in yeast and humans and hem12 yeast mutants mimic porphyria cutanea tarda (PCT), a hereditary human disease caused by mutations in the UROD gene. Even though mutations in other genes also affect UROD activity and predispose to sporadic PCT, the regulation of UROD is unknown. Here, we used yeast as a model to study regulation of Hem12 by ubiquitination and involvement of Rsp5 ubiquitin ligase in this process. We found that Hem12 is monoubiquitinated in vivo by Rsp5. Hem12 contains three conserved lysine residues located on the protein surface that can potentially be ubiquitinated and lysine K8 is close to the 36-LPEY-39 (PY) motif which binds WW domains of the Rsp5 ligase. The hem12-K8A mutation results in a defect in cell growth on a glycerol medium at 38°C but it does not affect the level of Hem12. The hem12-L36A,P37A mutations which destroy the PY motif result in a more profound growth defect on both, glycerol and glucose-containing media. However, after several passages on the glucose medium, the hem12-L36A,P37A cells adapt to the growth medium owing to higher expression of hem12-L36A,P37A gene and higher stability of the mutant Hem12-L36A,P37A protein. The Hem12 protein is downregulated upon heat stress in a Rsp5-independent way. Thus, Rsp5-dependent Hem12 monoubiquitination is important for its functioning, but not required for its degradation. Since Rsp5 has homologs among the Nedd4 family of ubiquitin ligases in humans, a similar regulation by ubiquitination might be also important for functioning of the human UROD.
    Źródło:
    Acta Biochimica Polonica; 2015, 62, 3; 509-515
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Pharmacological versus genetic inhibition of heme oxygenase-1 - the comparison of metalloporphyrins, shRNA and CRISPR/Cas9 system
    Autorzy:
    Mucha, Olga
    Podkalicka, Paulina
    Czarnek, Maria
    Biela, Anna
    Mieczkowski, Mateusz
    Kachamakova-Trojanowska, Neli
    Stepniewski, Jacek
    Jozkowicz, Alicja
    Dulak, Jozef
    Loboda, Agnieszka
    Powiązania:
    https://bibliotekanauki.pl/articles/1038402.pdf
    Data publikacji:
    2018
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    CRISPR/Cas9
    shRNA
    inhibitors
    heme oxygenase-1
    HO-1
    off-target
    Opis:
    Inhibition of heme oxygenase-1 (HO-1, encoded by HMOX1), a cytoprotective, anti-apoptotic and anti-inflammatory enzyme, may serve as a valuable therapy in various pathophysiological processes, including tumorigenesis. We compared the effect of chemical inhibitors - metalloporphyrins, with genetic tools - shRNA and CRISPR/Cas9 systems, to knock-down (KD)/knock-out (KO) HO-1 expression/activity. 293T cells were incubated with metalloporphyrins, tin and zinc protoporphyrins (SnPPIX and ZnPPIX, respectively) or were either transduced with lentiviral vectors encoding different shRNA sequences against HO-1 or were modified by CRISPR/Cas9 system targeting HMOX1. Metalloporphyrins decreased HO activity but concomitantly strongly induced HO-1 mRNA and protein in 293T cells. On the other hand, only slight basal HO-1 inhibition in shRNA KD 293T cell lines was confirmed on mRNA and protein level with no significant effect on enzyme activity. Nevertheless, silencing effect was much stronger when CRISPR/Cas9-mediated knock-out was performed. Most of the clones harboring mutations within HMOX1 locus did not express HO-1 protein and failed to increase bilirubin concentration after hemin stimulation. Furthermore, CRISPR/Cas9-mediated HO-1 depletion decreased 293T viability, growth, clonogenic potential and increased sensitivity to H2O2 treatment. In summary, we have shown that not all technologies can be used for inhibition of HO activity in vitro with the same efficiency. In our hands, the most potent and comprehensible results can be obtained using genetic tools, especially CRISPR/Cas9 approach.
    Źródło:
    Acta Biochimica Polonica; 2018, 65, 2; 277-286
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    HIF-1: the knowns and unknowns of hypoxia sensing.
    Autorzy:
    Zagórska, Anna
    Dulak, Józef
    Powiązania:
    https://bibliotekanauki.pl/articles/1041533.pdf
    Data publikacji:
    2004
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    angiogenesis
    prolyl and asparaginyl hydroxylases
    hypoxia inducible factor-1
    carbon monoxide
    reactive oxygen species
    nitric oxide
    heme oxygenase
    Opis:
    Hypoxia-inducible factor-1 (HIF-1) is a transcriptional activator that functions as a master regulator of cellular and systemic oxygen homeostasis. It consists of two constitutively produced subunits: HIF-1α and HIF-1β. Under normoxic conditions HIF-1α undergoes hydroxylation at specific prolyl residues which leads to an immediate ubiquitination and subsequent proteasomal degradation of the α subunit. Additionally, hydroxylation of an asparaginyl residue blocks the transcriptional activity of HIF-1 due to inhibition of its interaction with co-activators. In contrast, under hypoxic conditions, abolition of prolyl hydroxylation results in HIF-1α stabilization, whereas the lack of asparaginyl hydroxylation allows the transcriptional activity. Additionally, the transcriptional activity may be modulated by phosphorylation or redox modification of HIF-1. Despite its name, HIF-1 is induced not only in response to reduced oxygen availability but also by other stimulants, such as nitric oxide, various growth factors, or direct inhibitors of prolyl and asparaginyl hydroxylases. Therefore, it seems to be a crucial transcription factor elicited by a wide range of stresses such as impaired oxygenation, inflammation, energy deprivation, or intensive proliferation. However, the mechanisms of normoxic activation, as well as of oxygen sensing, are not yet fully known. Further understanding of the processes that control HIF-1 activity will be crucial for the development of new diagnostic and therapeutic strategies.
    Źródło:
    Acta Biochimica Polonica; 2004, 51, 3; 563-585
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Adult stem cells: hopes and hypes of regenerative medicine
    Autorzy:
    Dulak, Józef
    Szade, Krzysztof
    Szade, Agata
    Nowak, Witold
    Józkowicz, Alicja
    Powiązania:
    https://bibliotekanauki.pl/articles/1038957.pdf
    Data publikacji:
    2015
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    embryonic stem cells
    induced pluripotent stem cells
    myocardial infarction
    very small embryonic-like stem cells
    heme oxygenase-1
    Opis:
    Stem cells are self-renewing cells that can differentiate into specialized cell type(s). Pluripotent stem cells, i.e. embryonic stem cells (ESC) or induced pluripotent stem cells (iPSC) differentiate into cells of all three embryonic lineages. Multipotent stem cells, like hematopoietic stem cells (HSC), can develop into multiple specialized cells in a specific tissue. Unipotent cells differentiate only into one cell type, like e.g. satellite cells of skeletal muscle. There are many examples of successful clinical applications of stem cells. Over million patients worldwide have benefited from bone marrow transplantations performed for treatment of leukemias, anemias or immunodeficiencies. Skin stem cells are used to heal severe burns, while limbal stem cells can regenerate the damaged cornea. Pluripotent stem cells, especially the patient-specific iPSC, have a tremendous therapeutic potential, but their clinical application will require overcoming numerous drawbacks. Therefore, the use of adult stem cells, which are multipotent or unipotent, can be at present a more achievable strategy. Noteworthy, some studies ascribed particular adult stem cells as pluripotent. However, despite efforts, the postulated pluripotency of such events like "spore-like cells", "very small embryonic-like stem cells" or "multipotent adult progenitor cells" have not been confirmed in stringent independent studies. Also plasticity of the bone marrow-derived cells which were suggested to differentiate e.g. into cardiomyocytes, has not been positively verified, and their therapeutic effect, if observed, results rather from the paracrine activity. Here we discuss the examples of recent studies on adult stem cells in the light of current understanding of stem cell biology.
    Źródło:
    Acta Biochimica Polonica; 2015, 62, 3; 329-337
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Max Rudolf Lemberg (1896–1975) – australijski biochemik o wrocławskich korzeniach
    Max Rudolf Lemberg (1896–1975) – an australian biochemist of Wrocław origin
    Autorzy:
    Wojaczyński, J.
    Powiązania:
    https://bibliotekanauki.pl/articles/172331.pdf
    Data publikacji:
    2014
    Wydawca:
    Polskie Towarzystwo Chemiczne
    Tematy:
    chemicy australijscy
    chemicy niemieccy
    naukowcy urodzeni we Wrocławiu
    proces degradacji hemu
    chemia barwników żółciowych
    Austalian chemists
    German chemists
    scientists born in Wrocław
    heme degradation process
    bile pigments chemistry
    Opis:
    The article is devoted to Max Rudolf Lemberg (1896–1975), known primarily as an author of pioneering works on bile pigments and porphyrin degradation (in particular, coupled oxidation), and to his connections with Wrocław. This Australian biochemist of German origin was born in that city to an assimilated Jewish family. He was educated by a private teacher, and in 1905 he entered the famous liberal Johannes Gymnasium in Breslau (its building now houses Economics and Administration Schools). After leaving school in 1914, shortly before the war broke out, Lemberg began studies on natural sciences at the University of Breslau. He volunteered for an army, but was not accepted until 1917. Wounded in the Somme offensive in 1918, he resumed his studies to finish with a doctorate on the chemistry of uric acid derivatives (1921). He then became a private assistant to his Ph.D. supervisor, Professor Heinrich Biltz. However, a few years later, Biltz advised him to look for a job in the industry, and Lemberg moved to Meinheim to work for a pharmaceutical company. He often visited his native city where his parents and brother were living; in Breslau he also married Hanna Clausen in 1924. A grant from Notgemeinschaft der Deutschen Wissenschaft and job offer from Karl Freudenberg of University of Heidelberg allowed Lemberg to come back to the scientific work, in which he decided to focus on biochemical studies. From these days dates his interest in bile pigments which led him to the habilitation in 1930. He then continued his work on linear tetrapyrroles during Rockefeller Foundation Fellowship in Cambridge. Shortly after his return to Heidelberg, Nazis came to power in Germany and proclaimed the Beamtengesetz act which stated that all people of Jewish origin as well as members and supporters of opposition parties should be fined from the civil service. This ended his academic career of Lemberg in Germany. Rudolf moved to Cambridge with Hanna, however, since not all refugees could stay in the Great Britain, in 1935 he accepted a proposal from the Royal North Shore Hospital in Sydney to work as a research biochemist. The Lembergs immigrated to Australia to begin the new chapter in their life; a few years later Walter, Rudolph’s brother, joined them with his family. The first years were particularly hard since the progress in the scientific work was hampered by the lack of modern laboratory equipment and experienced coworkers. In 1946, first of Lemberg’s books, Hematin Compounds and Bile Pigments, co-authored by John Legge, was issued. In the following years, Rudolf broadened his interests to cytochrome c oxidase and heme A, one of the enzyme prosthetic groups. His investigations in the field were summarized in the second monograph written with Jack Barrett („The Cytochromes”, 1973). His scientific interests were not limited to chemistry: he devoted several papers and lectures to the problem of life origins and to the connections between religion and science. Rudolf Lemberg was one of the founders of Australian Academy of Sciences and Australian Biochemical Society. He died in Sydney in 1975.
    Źródło:
    Wiadomości Chemiczne; 2014, 68, 11-12; 1095-1111
    0043-5104
    2300-0295
    Pojawia się w:
    Wiadomości Chemiczne
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Therapeutic potential of heme oxygenase-1 in cardiovascular disease
    Autorzy:
    Jazwa, A.
    Florczyk, U.
    Stepniewski, J.
    Jozkowicz, A.
    Dulak, J.
    Powiązania:
    https://bibliotekanauki.pl/articles/80176.pdf
    Data publikacji:
    2011
    Wydawca:
    Polska Akademia Nauk. Czytelnia Czasopism PAN
    Tematy:
    angiogenesis
    angiogenic factor
    antiapoptotic effect
    antiinflammatory effect
    antioxidant effect
    carbon monoxide
    cardiovascular disease
    cytoprotection
    endothelial cell
    ferrous iron
    heme oxygenase-1
    hypoxia
    iron
    stem cell
    stromal cell
    therapeutic potential
    vascular endothelial growth factor-A
    Źródło:
    BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2011, 92, 2
    0860-7796
    Pojawia się w:
    BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
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